Canonical Allele Identifier: CA372291995

Gene: DNAAF11

Linked Data

• MyVariant Identifiers: chr8:g.133584704T>G (hg19) ; chr8:g.132572456T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132572456T>G , CM000670.2:g.132572456T>G	GRCh38
NC_000008.10:g.133584704T>G , CM000670.1:g.133584704T>G	GRCh37
NC_000008.9:g.133653886T>G	NCBI36
NG_033068.1:g.108160A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000620350.5:c.1251A>C MANE Select	ENSP00000484634.1:p.Glu417Asp
ENST00000250173.5:c.*115A>C	ENSP00000250173.2:n.*115A>C
ENST00000518642.5:c.*115A>C	ENSP00000428610.1:n.*115A>C
ENST00000519595.5:c.1251A>C	ENSP00000429791.1:p.Glu417Asp
ENST00000522597.1:n.520A>C
ENST00000522789.5:c.471A>C	ENSP00000428015.1:p.Glu157Asp
ENST00000618342.1:c.1251A>C	ENSP00000484802.1:p.Glu417Asp
ENST00000620350.4:c.1251A>C	ENSP00000484634.1:p.Glu417Asp
NM_012472.4:c.1251A>C	NP_036604.2:p.Glu417Asp
NR_073525.1:n.1475A>C
XM_006716538.2:c.1269A>C	XP_006716601.2:p.Glu423Asp
XM_011516950.1:c.1209A>C	XP_011515252.1:p.Glu403Asp
XM_011516952.1:c.1005A>C	XP_011515254.1:p.Glu335Asp
XM_011516953.1:c.891A>C	XP_011515255.1:p.Glu297Asp
XM_011516954.1:c.891A>C	XP_011515256.1:p.Glu297Asp
XR_428377.2:n.1503A>C
NM_001321961.1:c.1191A>C	NP_001308890.1:p.Glu397Asp
NM_001321962.1:c.1005A>C	NP_001308891.1:p.Glu335Asp
NM_001321963.1:c.891A>C	NP_001308892.1:p.Glu297Asp
NM_001321964.1:c.891A>C	NP_001308893.1:p.Glu297Asp
NM_001321965.1:c.891A>C	NP_001308894.1:p.Glu297Asp
NM_001321966.1:c.831A>C	NP_001308895.1:p.Glu277Asp
NM_012472.5:c.1251A>C	NP_036604.2:p.Glu417Asp
NR_073525.2:n.1475A>C
NR_135905.1:n.1464A>C
NR_135906.1:n.905A>C
NR_135907.1:n.1151A>C
NR_135908.1:n.845A>C
NR_135909.1:n.1269A>C
NR_135910.1:n.1576A>C
NR_135911.1:n.1655A>C
NR_135912.1:n.2214A>C
NR_135913.1:n.1901A>C
XM_006716538.3:c.1269A>C	XP_006716601.2:p.Glu423Asp
XM_011516950.2:c.1209A>C	XP_011515252.1:p.Glu403Asp
XM_017013296.1:c.1149A>C	XP_016868785.1:p.Glu383Asp
XM_017013297.1:c.891A>C	XP_016868786.1:p.Glu297Asp
XM_017013298.1:c.891A>C	XP_016868787.1:p.Glu297Asp
NM_012472.6:c.1251A>C MANE Select	NP_036604.2:p.Glu417Asp
NM_001321961.2:c.1191A>C	NP_001308890.1:p.Glu397Asp
NM_001321962.2:c.1005A>C	NP_001308891.1:p.Glu335Asp
NM_001321963.2:c.891A>C	NP_001308892.1:p.Glu297Asp
NM_001321964.2:c.891A>C	NP_001308893.1:p.Glu297Asp
NM_001321965.2:c.891A>C	NP_001308894.1:p.Glu297Asp
NM_001321966.2:c.831A>C	NP_001308895.1:p.Glu277Asp
NR_073525.3:n.1403A>C
NR_135905.2:n.1392A>C
NR_135906.2:n.833A>C
NR_135907.2:n.1079A>C
NR_135908.2:n.773A>C
NR_135909.2:n.1289A>C
NR_135910.2:n.1639A>C
NR_135911.2:n.1759A>C
NR_135912.2:n.2318A>C
NR_135913.2:n.2005A>C